IDEXX Laboratories
Veteriner teşhisleri, analizörleri ve hayvan sağlığı test ürünleri.
IDEXX Laboratuvarları, Westbrook operasyonlarından veteriner teşhis cihazları, analiz cihazları ve hayvan sağlığı test ürünleri üretmektedir. Şirket, listelenen birincil pazarlarda sağlık sistemleri, laboratuvarlar, OEM ortakları veya düzenlemeye tabi ihracat müşterilerine hizmet vermektedir.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Westbrook, United States
- Founded
- 1983
- Website
- idexx.com
- Categories
- Tıbbi ve Sağlık Malzemeleri, Evcil Hayvan Bakımı ve Aksesuarları
- Markets
- Amerika Birleşik Devletleri, Almanya, Japonya, Avustralya
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- domain-registered (green), checked 2026-08-08 Domain registry record
- market-access-eu (green), checked 2026-08-22 TRACES NT, European Commission register of approved establishments (DG SANTE)
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- facility-registered (green), effective since 2026-08-07 US EPA Facility Registry Service (national combined file)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- industrial-permit (green), checked 2026-08-23 ECHO, Enforcement and Compliance History Online (U.S. Environmental Protection Agency)
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Consumer goods sold in the EU fall under the General Product Safety Regulation (GPSR, applies since 13 Dec 2024): a responsible person in the EU is mandatory. EUR-Lex: Regulation (EU) 2023/988 (GPSR)